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The dual-specificity MAP kinase phosphatases: critical roles in development and cancer

Bermudez, O., Pagès, G., Gimond, C.·2010·American Journal of Physiology-Cell Physiology

Abstract

Intracellular signaling by mitogen-activated protein (MAP) kinases (MAPK) is involved in many cellular responses and in the regulation of various physiological and pathological conditions. Tight control of the localization and duration of extracellular-regulated kinase (ERK), c-Jun NH 2-terminal kinase (JNK), or p38 MAPK activity is thus a fundamental aspect of cell biology. Several members of the dual-specificity phosphatase (DUSPs) family are able to dephosphorylate MAPK isoforms with different specificity, cellular, and tissue localization. Understanding how these phosphatases are themselves regulated during development or in physiological and pathological conditions is therefore fundamental. Over the years, gene deletion and knockdown studies have completed initial in vitro studies and shed a new light on the global and specific roles of DUSPs in vivo. Whereas DUSP1, DUSP2, and DUSP10 appear as crucial players in the regulation of immune responses, other members of the family, like the ERK-specific DUSP6, were shown to play a major role in development. Recent findings on the involvement of DUSPs in cancer progression and resistance will also be discussed.

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Metadata

Authors
Bermudez, O., Pagès, G., & Gimond, C.
Venue
American Journal of Physiology-Cell Physiology
Published
2010-08
Volume
299
Issue
2
Pages
C189-C202
ISSN
  • 0363-6143 (ISSN-L)
  • 1522-1563
OpenAlex
W2071900417
Cited by
230
References
11
FWCI
7.92
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The dual-specificity MAP kinase phosphatases: critical roles in development and cancer. https://app.cochat.ai/papers/10.1152/ajpcell.00347.2009
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Bermudez, O., Pagès, G., & Gimond, C. (2010). The dual-specificity MAP kinase phosphatases: critical roles in development and cancer. American Journal of Physiology-Cell Physiology. https://doi.org/10.1152/ajpcell.00347.2009

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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